Search Results - "Buchmayer, H"

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  1. 1

    Erythropoietin-inducible immediate-early genes in human vascular endothelial cells by Födinger, M, Fritsche-Polanz, R, Buchmayer, H, Skoupy, S, Sengoelge, G, Hörl, W H, Sunder-Plassmann, G

    Published in Journal of investigative medicine (01-03-2000)
    “…Patients receiving recombinant human erythropoietin (rHuEPO) may experience side effects arising from the vascular system. The underlying mechanisms, however,…”
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    Journal Article
  2. 2

    Molecular genetic differentiation between primary lung cancers and lung metastases of other tumors by Kandioler, Daniela, Dekan, Gerhard, End, Adelheid, Paschinga, Eva, Buchmayer, Heidi, Gnant, Michael, Langmann, Florian, Mannhalter, Christine, Eckersberger, Franz, Wolner, Ernst

    “…When solitary pulmonary tumors are observed in patients with a history of cancer, differentiation between metastasis and primary lung cancer is crucial for…”
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    Journal Article
  3. 3

    Citrate for long-term hemodialysis: Prospective study of 1,009 consecutive high-flux treatments in 59 patients by Apsner, Robert, Buchmayer, Heidi, Gruber, Diego, Sunder-Plassmann, Gere

    Published in American journal of kidney diseases (01-03-2005)
    “…Background: Regional citrate anticoagulation during hemodialysis is performed in selected patients at highly specialized units. We postulated that routine use…”
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    Journal Article
  4. 4

    Effect of high dose folic acid therapy on hyperhomocysteinemia in hemodialysis patients : Results of the Vienna multicenter study by SUNDER-PLASSMANN, G, FÖDINGER, M, AUINGER, M, BARNAS, U, HÖRL, W. H, BUCHMAYER, H, PAPAGIANNOPOULOS, M, WOJCIK, J, KLETZMAYR, J, ENZENBERGER, B, JANATA, O, WINKELMAYER, W. C, PAUL, G

    “…Homocysteine is associated with atherosclerosis and enhanced cardiovascular risk. In previous studies, treatment with folic acid up to 15 mg/d failed to…”
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    Journal Article
  5. 5

    Simplified citrate anticoagulation for high-flux hemodialysis by Apsner, Robert, Buchmayer, Heidi, Lang, Thomas, Unver, Beate, Speiser, Wolfgang, Sunder-Plassmann, Gere, Hörl, Walter H.

    Published in American journal of kidney diseases (01-11-2001)
    “…In a randomized crossover trial, we compared a simple citrate anticoagulation protocol for high-flux hemodialysis with standard anticoagulation by…”
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    Journal Article
  6. 6
  7. 7

    Efficacy of folinic versus folic acid for the correction of hyperhomocysteinemia in hemodialysis patients by Hauser, Anna-Christine, Hagen, Wolfgang, Rehak, Peter H., Buchmayer, Heidi, Födinger, Manuela, Papagiannopoulos, Menelaos, Bieglmayer, Christian, Aspner, Robert, Köller, Elke, Ignatescu, Mihaela, Hörl, Walter H., Sunder-Plassmann, Gere

    Published in American journal of kidney diseases (01-04-2001)
    “…The effectiveness of intravenous folinic acid or intravenous folic acid for the treatmentof hyperhomocysteinemia of hemodialysis patients is unknown. In a…”
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    Journal Article Conference Proceeding
  8. 8

    Association of two MTHFR polymorphisms with total homocysteine plasma levels in dialysis patients by Födinger, Manuela, Buchmayer, Heidi, Heinz, Gotfried, Papagiannopoulos, Menelaos, Kletzmayr, Josef, Perschl, Agnes, Vychytil, Andreas, Hörl, Walter H., Sunder-Plassmann, Gere

    Published in American journal of kidney diseases (01-07-2001)
    “…The effect of the combined 5,10-methylenetetrahydrofolate reductase (MTHFR) 677C→T and 1298A→C genotype on total homocysteine (tHcy), folate, and vitamin B12…”
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    Journal Article
  9. 9

    Effect of MTHFR genotypes and hyperhomocysteinemia on patient and graft survival in kidney transplant recipients by Hagen, W, Födinger, M, Heinz, G, Buchmayer, H, Hörl, W H, Sunder-Plassmann, G

    Published in Kidney international (01-02-2001)
    “…The total homocysteine (tHcy) plasma level, which is partly determined by the MTHFR 677C-->T genotype, may be associated with vascular disease. We…”
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    Journal Article
  10. 10

    High prevalence of hyperhomocysteinemia in critically ill patients by Schindler, Karin, Zauner, Christian, Buchmayer, Heidi, Födinger, Manuela, Wölfl, Gabriele, Bieglmayer, Christian, Heinz, Gottfried, Wilfing, Astrid, Hörl, Walter H, Sunder-Plassmann, Gere

    Published in Critical care medicine (01-04-2000)
    “…OBJECTIVE:To test the hypothesis that the prevalence of hyperhomocysteinemia is increased in critically ill patients and correlates with disease severity and…”
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    Journal Article
  11. 11

    G-protein beta3 subunit gene (GNB3) polymorphism 825C-->T in patients with hypertensive crisis by Buchmayer, H, Sunder-Plassmann, G, Hirschl, M M, Kletzmayr, J, Woisetschläger, C, Laggner, A N, Hörl, W H, Födinger, M

    Published in Critical care medicine (01-09-2000)
    “…The polymorphism 825C-->T in exon 10 of the gene GNB3 encoding the beta3 subunit of heterotrimeric guanine nucleotide binding regulatory proteins (G-proteins)…”
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    Journal Article
  12. 12

    Multiplex PCR for rapid detection of T-cell receptor-gamma chain gene rearrangements in patients with lymphoproliferative diseases by Födinger, M, Buchmayer, H, Schwarzinger, I, Simonitsch, I, Winkler, K, Jäger, U, Knobler, R, Mannhalter, C

    Published in British journal of haematology (01-07-1996)
    “…We describe a multiplex polymerase chain reaction (PCR) method suitable for the detection of all T-cell receptor (TCR) gamma-chain gene rearrangements in…”
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    Journal Article
  13. 13

    Molecular genetics of homocysteine metabolism by Födinger, M, Buchmayer, H, Sunder-Plassmann, G

    Published in Mineral and electrolyte metabolism (01-07-1999)
    “…Recent genetic studies have led to the characterization of molecular determinants contributing to the pathogenesis of hyperhomocysteinemia. In this article we…”
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    Journal Article
  14. 14

    Identification of a variable number tandem repeat region in the human T cell receptor alpha-delta (TCRAD) locus by BUCHMAYER, H, RUMPOLD, H, MANNHALTER, C

    Published in Human genetics (01-09-1996)
    “…A number of different polymorphisms have been observed in coding as well as in non-coding regions of T cell receptor (TCR) genes. We report the identification…”
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    Journal Article
  15. 15

    Molecular and clinical characterisation of homocystinuria in two Austrian families with cystathionine beta-synthase deficiency by Tröndle, U, Sunder-Plassmann, G, Burgmann, H, Buchmayer, H, Kramer, L, Bieglmayer, C, Hörl, W H, Födinger, M

    Published in Acta medica Austriaca (01-01-2001)
    “…The influence of the genotype on the phenotypic expression of homocystinuria due to cystathionine beta-synthase (CBS) deficiency is frequently unclear. We…”
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    Journal Article
  16. 16